Who we are


Alopecia Areata: The shame and embarrassment of this disease devastates the lives of too many women and girls when treatments do not work. Since 2007 Bald Girls Do Lunch has connected with over 3,000 to restore self-confidence and conquer isolation. With requests for meet-ups in every state and beyond the USA, Bald Girls is answering the plea for women to find others for community and support. From intimate groups to style workshops to restoring her looks, BGDL puts women on the track to normalcy and living well with this disease. Learn more...

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Posts


Talk to the FDA! Alopecia Areata Patient Views Needed

November 12th, 2017 by Chassin

FDA

Our submissions page to Talk to the FDA via the Bald Girls Do Lunch impact statement is now closed.

You may enter your comments through 11:59 pm eastern, November 13, 2017 directly to the FDA here.


Drawing on Eyebrows Tutorial with Laura Latti

September 26th, 2017 by Christie Plummer

Alopecia beauty vlogger Laura Latti gives a tutorial on drawing eyebrows using BG Brows Sealant + Dollywink Liquid Eyeliner.


Alopecia Makeup Review with Alopecia Beauty Vlogger Laura Latti

August 31st, 2017 by Chassin



Beauty alopecia vlogger Laura Latti gives BGBrows.com makeup the all-day test.


Alopecia Support with Bald Girls Do Lunch Changed My Life!

April 27th, 2017 by Chassin

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Alopecia Support in Boston

June 6th, 2016 by Chassin

Alopecia Support in Boston

 

June 13, 2016: 6 pm

Boston Renaissance Waterfront Hotel | 606 Congress St, Boston, MA

  • • Registration required.
  • • Includes one raffle for a wig from Fortune Wigs.
  • • Early bird discount: offer code BOSTON for $5 off until June 7th
  • • Questions? info@BaldGirlsDoLunch.org or 800.578.5332

Come to talk and share.

Our useful tips help you today.

 

Feeling Lost?

Enjoy our fun approach to self-confidence.

 

We love options. Come as you are.

All looks encouraged.

 

 

 


Visit the AA Support Blog for Research News and More!

December 10th, 2014 by Chassin

We’ve got original features on clinical trials, personal stories and tips to live well with alopecia.  Check out BGDL’s Alopecia Areata Support Network blog!

Visit Now

 

 


Different Perspectives: Sharing your Alopecia Story with Friends

November 6th, 2014 by Chassin

 

Very recently while speaking with one of my cherished childhood friends, she told me about a friend of hers that she suspects has the condition. I wanted to hear her advice for men and women like her friend who have never mentioned why they look the way they do.

Read the full article here:

 

Sign up for weekly updates here.

 


The Importance of Talking About Alopecia Areata

October 30th, 2014 by Chassin

 

As we approach the holiday season when folks are gathering ’round, we want to help this be a better year for women with alopecia areata.

Read the full article here:

 

Sign up for weekly updates here.

 


Research News You Can Use from BGDL

October 23rd, 2014 by Chassin

 

 

We’ve recently focused on the latest medicines and research in the alopecia areata field. Interested in the latest science and findings?

Read the full articles here:

 

Sign up for weekly updates here.